Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing-Reference-Cited by-同舟云学术

Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing

Author:

Cromer M. Kyle¹,Starker Lee F.²³,Choi Murim¹,Udelsman Robert²,Nelson-Williams Carol¹,Lifton Richard P.¹,Carling Tobias²⁴⁵

Affiliation:

1. Departments of Genetics (M.K.C., M.C., C.N.-W., R.P.L.), New Haven, Connecticut 06520

2. Surgery (L.F.S., R.U., T.C.), New Haven, Connecticut 06520

3. Department of Surgical Sciences (L.F.S.), Uppsala University, SE-751 85 Uppsala, Sweden

4. Yale Endocrine Neoplasia Laboratory (L.F.S., T.C.), New Haven, Connecticut 06520

5. Cancer Genetics and Genomics Program (T.C.), Yale Cancer Center, Yale University School of Medicine, New Haven, Connecticut 06520

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

Reference48 articles.

2. Parathyroid “double adenomas”: fact or fiction?;Verdonk;Surgery,1981

5. Novel chromosomal abnormalities identified by comparative genomic hybridization in parathyroid adenomas.;Palanisamy;J Clin Endocrinol Metab,1998

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